Double-perovskite magnetic La2NiMnO6 nanoparticles for adsorption of bovine serum albumin applications
© Wu et al.; licensee Springer. 2013
Received: 13 March 2013
Accepted: 20 April 2013
Published: 2 May 2013
Double-perovskite La2NiMnO6 (LNMO) nanoparticles were synthesized by co-precipitation process, and the adsorption of bovine serum albumin (BSA) protein on these nanoparticles was carried out. The powder samples were annealed at 750, 850, 950, and 1,050°C, respectively. X-ray diffraction (XRD) results reveal that there are double perovskites and exhibit mixed orientations, without any impurity phases. Transmission electron microscopy results as well as the XRD estimate results show that the crystalline size is about 34 to 40 nm. The adsorption of BSA on the magnetic nanoparticles was analyzed using a UV spectrophotometer at room temperature. The results show that the as-prepared LNMO nanoparticles display a good adsorbing ability for BSA, and the nanoparticle sintered at 850°C has the highest value of 219.6 mg/g, which is much higher than others.
KeywordsChemical co-precipitation LNMO Magnetic property Nanoparticles Adsorption Bovine serum albumin protein
Magnetic nanoparticles are commercially important materials as a consequence of their stability and striking magnetic property  and are applied widely in biological and medical areas, such as bioseparation , drug and gene delivery , quantitative immunoassay , and hyperthermia .
Recently, magnetic nanoparticles, such as CoFe2O4, MnFe2O4, Fe2O3, Fe3O4, and Fe [6–10], have been studied mostly for biomedical applications, but the application of double-perovskite La2NiMnO6 nanoparticles in biomedical has not been reported. Double-perovskite La2NiMnO6 is a ferromagnetic material and attractive due to its impressive properties. In order to be applied in biological and medical fields, La2NiMnO6 nanoparticles should be monodispersed to bind biomolecules. Proteins are relatively large biomolecules and usually have a tendency to accumulate at the interface between aqueous solutions and solid surfaces [11–15]. Protein adsorption to surfaces is important in many disciplines, including biomedical engineering, biotechnology, and environmental science.
Many works were used to research the magnetic characteristics of double-perovskite nanoparticles. There has been no report about the application of these nanoparticles in biomedicine. Our experiments show that different annealing temperatures can affect the adsorbing ability for bovine serum albumin (BSA). In this paper, we report that the monodispersed La2NiMnO6 nanoparticles were synthesized by co-precipitation, and the magnetic properties and adsorption characteristics of bovine serum albumin for these nanoparticles were analyzed.
The La2NiMnO6 (LNMO) nanocomposites were synthesized by co-precipitation, using La(NO3)3·5H2O(99.5%), Ni(CH3COO)2·4H2O (98%), and Mn(CH3COO)4·4H2O(99%) as starting raw materials . The raw powders were dissolved in deionized water in required stoichiometric proportions. The solutions were then poured together into a beaker and stirred in a magnetic blender at 80°C. After 2 h, aqueous ammonia solution was added to the container until a brown suspension took shape at a pH of approximately 8.5 . After stirring for about 30 min, the suspension was ball-milled for 24 h with ethanol as a milling medium in order to mix the reactants well enough and then dried in a cabinet dryer at 80°C overnight to obtain the precursor samples. The dried powders were finally annealed in nitrogen atmosphere for 2 h at different temperatures in the range of 750°C~1,050°C.
The crystalline phase of LNMO nanocomposites was identified using the X-ray diffraction (XRD) technique. The X-ray diffractogram of all the samples from 10° to 70° at a scanning step of 0.02°/s was recorded using a Rigaku X-ray diffractometer (Rigaku Corporation, Tokyo, Japan) with Cu Kα radiation (λ = 1.54056 Ǻ ). The magnetic properties were measured using a vibrating sample magnetometer (PPMS-9, Quantum Design, Inc., San Diego, CA, USA) at room temperature under a maximum field of 30 kOe. The structural defects in the LNMO materials were investigated using a JEOL 4000EX high-resolution transmission electron microscope (HRTEM; JEOL Ltd., Tokyo, Japan) operated at 400 kV. The adsorption of BSA protein on nanoparticles was analyzed with a UV spectrophotometer (UV-2401 PC, Shimadzu Corporation, Kyoto, Japan) at room temperature. The aqueous solution with a pH of about 7.4 contained 1.000 mg/ml BSA (purity >99%) before the adsorption, and for each measurement, 3.00 to 12.00 mg of La(Ni0.5Mn0.5)O3 nanoparticles was used as the adsorbent. The adsorbent was stirred ultrasonically in the BSA solution for 1 h at room temperature, which was put in static precipitation condition after 12 h to be measured.
Results and discussion
Average grain size and magnetic and BSA adsorption properties of La(Ni 0.5 Mn 0.5 )O 3 nanoparticles
Annealing temperature (°C)
Grain size (nm)
Nanoparticle mass (mg)
BSA adsorbed (mg/g)
LaMnO3 is an ABO3 perovskite ferromagnetic material. The ionic radius of Ni3+ (62 pm) is smaller than that of Mn3+ (66 pm). Therefore, an inhomogeneous distribution results at the B site of the structure. A cationic disorder induced by B-site substitution is always regarded as the main derivation of crystalline growth. On the other hand, LaNiO3 is a paramagnetic material; the La ion locates at the central equilibrium position of the LaNiO3 lattice. In this case, the macrodomain in LaMnO3 could be divided into the microdomains which probably cause the crystalline growth. Because the domain size relates to the grain sizes, the grain size increases slowly when the annealing temperature increases.
where η indicates the amount of 1-mg nanoadsorbents (mg/g) in the adsorbed BSA, mBSA is the total weight of BSA (mg), mmag is the dry weight of nanopowders used to bind BSA (mg), ABSA points to the UV absorbance value of the blank BSA solution, and Amag refers to the UV absorbance value of the supernatant after adsorption.
Adsorption of bovine serum albumin on LNMO nanoparticles
BSA is a globular protein with the approximate shape of a prolate spheroid with dimensions of 4 nm × 4 nm × 14 nm . Table 1 shows BSA adsorption on the LNMO nanoparticles. From Table 1, it can be seen that the LNMO nanoparticles exhibit a good absorbing characteristic for BSA protein. The BSA adsorption capability on the LNMO nanoparticles is influenced possibly by their grain size, specific surface area, magnetic properties, interface structure, the electrostatic attraction between BSA and magnetic nanoparticles, etc., which are related to the preparation process. The LNMO nanoparticles annealed at 850°C show the highest BSA adsorption at around 219.6 mg/g. On this circumstance, the volume of the aqueous BSA solution after adsorption was increased to about 3 ml. The LNMO nanoparticles annealed at 850°C showed the lowest coercive field (19.9 Oe, see Table 1) and have the highest BSA adsorption at around 219.6 mg/g; the main reason is based on the critical grain size of LNMO nanoparticles for BSA adsorption.
The reason for this is not clear, and it needs a further systematic study. In fact, up to now, protein adsorption mechanism on nanoparticles is not fully understood although it has been intensively investigated by researchers [24, 25].
In conclusion, La(Ni0.5Mn0.5)O3 (LNMO) nanoparticles have been successfully prepared using the chemical co-precipitation process. The grain size and magnetic properties of the LNMO nanoparticles are largely influenced by annealing temperature. As the annealing temperature increases from 750°C to 1,050°C, the average grain size increases from about 33.9 to 39.6 nm, respectively. The saturation magnetization increases from about 35.95 to 67.19 emu/g; However, as the annealing temperature increases from 950°C to 1,050°C, the average grain size decreases from about 37.9 to 39.6 nm, and the saturation magnetization decreases from about 1.97×10-3 to 3.79×10-3 emu/g. On the other hand, the coercivity initially increases, reaching a maximum value of 42.3 Oe when the average grain size is about 37.9 nm at 950°C, and then reduces. The LNMO nanoparticles showed good adsorption performance in bovine serum albumin protein, and the preliminary optimized adsorption is obtained for the LNMO nanoparticles annealed at 850°C. These LNMO nanoparticles are a potential carrier for large biomolecules, which will be widely used in the biomedical field.
This work was supported by the National Natural Science Foundation of China (grant nos. 10774030 and 11032010), the Guangdong Provincial Natural Science Foundation of China (Grant Nos. 8151009001000003 and 10151009001000050), and the Guangdong Provincial Educational Commission of China (No. 2012KJCX0044).
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